QA Specialist I: GMP Batch Release & Compliance

A leading biotechnology firm is seeking a QA Specialist I to ensure compliance with regulatory standards. The ideal candidate will have a Bachelor’s Degree in Science and a minimum of 2 years in biotechnology manufacturing. Responsibilities include auditing batch records, preparing compliance reports, and participating in plant meetings. Excellent communication skills in English and Spanish are necessary, along with proficiency in SAP, LIMS, and MES. This position is based in Puerto Rico and offers a structured work schedule from Monday to Friday, 8 AM to 5 PM. #J-18808-Ljbffr